1-Acetyladamantane

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Names

[ CAS No. ]:
1660-04-4

[ Name ]:
1-Acetyladamantane

[Synonym ]:
1-Acetyladamantane
Methyl 1-mdamantyl ketone
1-Adamantan-1-ylethanone
MFCD00074739
Ethanone, 1-tricyclo[3.3.1.1]dec-1-yl-
1-Acetyl Adamantane
1-Adamantyl methyl ketone
Methyl 1-Adamantyl Ketone
1-(1-adamantyl)ethan-1-one
EINECS 216-761-9
1-(Adamantan-1-yl)ethanone

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
262.3±8.0 °C at 760 mmHg

[ Melting Point ]:
53-55 °C(lit.)

[ Molecular Formula ]:
C12H18O

[ Molecular Weight ]:
178.271

[ Flash Point ]:
107.4±6.1 °C

[ Exact Mass ]:
178.135757

[ PSA ]:
17.07000

[ LogP ]:
2.73

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.533

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914299000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1-(1-adamantyl)ethene
  • Methylmagnesium chloride
  • N-Methoxy-N-methyl-1-adamantanecarboxamide
  • 2,5-dimethyl-2-(1-adamantyl)-1,3-dioxolan-4-one
  • 5-bromo-2,5-dimethyl-2-(1-adamantyl)-1,3-dioxolan-4-one
  • Adamantane-1-carboxylic acid
  • METHYLLITHIUM
  • Adamantane
  • butane-2,3-dione

DownStream

  • Phenylacetic acid
  • {2-[2-(1-adamantyl)-2-oxoethyl]phenyl}acetic acid
  • 1-Adamantyl bromomethyl ketone
  • 1-acetyl-3-hydroxyadamantane
  • 1-acetamidoadamantane
  • Adamantane-1-carboxylic acid
  • Ethyl 1-adamantanecarboxylate
  • 1-(1'-chloroethenyl)adamantane
  • 2-(1-Adamantyl)-2-propanol

Customs

[ HS Code ]: 2914299000

[ Summary ]:
2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Stereoselective ketone reduction by a carbonyl reductase from Sporobolomyces salmonicolor. Substrate specificity, enantioselectivity and enzyme-substrate docking studies.

Org. Biomol. Chem. 4(14) , 2690-5, (2006)

In our effort to search for effective carbonyl reductases, the activity and enantioselectivity of a carbonyl reductase from Sporobolomyces salmonicolor have been evaluated toward the reduction of a va...


More Articles

Related Compounds

  • 1-ACETYLADAMANTANE
  • 4-hydroxy-1-acetyladamantane
  • 1-Acetyladamantane Intermediate
  • 1-methyl-3-[3-[[methyl-[(4-nitrophenyl)methyl]carbamoyl]amino]phenyl]-1-[(4-nitrophenyl)methyl]urea
  • 1-bromo-2,5-bis(chloromethyl)-4-methyl-benzene
  • 1,2,3,4,5-pentaphenylbenzene